Altalube
- Product NDC
- 59390-198
- 11-digit product format
- 593900198
- Labeler code
- 59390
- Product ID
- 59390-198_0c0e9c0d-6205-e63b-e063-6294a90ac0d9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Mineral oil and petrolatum
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Altaire Pharmaceuticals Inc.
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2002-02-01
- Substance
- MINERAL OIL; PETROLATUM
- Active strength
- 150; 850 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Altalube
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINERAL OIL | 150 mg/g |
| PETROLATUM | 850 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | T5L8T28FGP, 4T6H12BN9U |
| Rxcui | 579996, 1088146 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59390-198-50 | Altalube | 1 in 1 CARTON | OINTMENT | 1 | | 4 |
| 59390-198-50 | Altalube | 3.5 g in 1 TUBE | OINTMENT | 3.5 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59390-198 | ALTALUBE (MINERAL OIL AND PETROLATUM) OINTMENT [ALTAIRE PHARMACEUTICALS INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20231214_eb65004c-c3a7-4079-bd75-f2857d30c68a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59390-198-50 | 59390019850 | 1 TUBE in 1 CARTON (59390-198-50) / 3.5 g in 1 TUBE | 1 tube | 2002-02-01 | 0000-00-00 | No | No | Current |